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glycerol kinase deficiency
Summary
- Definition
- An inherited metabolic disorder characterized_by wide range of phenotypic variability; patients can have severe metabolic and CNS abnormalities, while others possess hyperglycerolemia and glyceroluria with no other apparent phenotype and that has_material_basis_in mutation in the GK gene on chromosome Xp21.
- Super Class
- inherited metabolic disorder
External Links
- Disease Ontology
- DOID:0060363
- Mondo Disease Ontology
- UMLS
- ORDO
- OMIM
- MGI genotype (from TogoID)
Related Genes
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001943 | Hypoglycemia |
| HP:0006280 | Chronic pancreatitis |
| HP:0001250 | Seizure |
| HP:0002714 | Downturned corners of mouth |
| HP:0000486 | Strabismus |
| HP:0002018 | Nausea |
| HP:0003560 | Muscular dystrophy |
| HP:0001419 | X-linked recessive inheritance |
| HP:0000316 | Hypertelorism |
| HP:0002155 | Hypertriglyceridemia |
